On Monday, April 29th, I was diagnosed with stage four Adenocarcinoma gastric cancer.

Today, Friday, May 10th, is my first day of Chemotherapy.

In a span of two weeks, everything has changed. It’s impossible to quantify. It’s impossible to feel.

Since February, I have been having digestive issues. There were issues with certain foods, a complete loss of appetite, really bad indigestion and cases of having trouble swallowing. Things came to a head in early April when I was in Chicago and I could not keep down any solid foods. If I managed to swallow even a tomato slice, or a spoonful of chicken, my body cratered to energy levels that could be labeled as zombie-like.

It turns out that these health concerns were valid.

After an endoscopy, CT Scans, multiple Emergency Department visits, X-Rays, MRIs, far too many catheter insertions, and infinite questionnaires, the rather depressing results are in.

I have cancer in my stomach, and my liver. All of it is too large to operate surgically. It’s too baked in.

According to the doctors at Sloan, the cancer I have is not curable. It’s something that can go away, but it’s something that I’ll have to monitor for the rest of my life.

There is also a hard truth. With what the doctors have been able to see thus far, if I do not respond to the Chemotherapy well, then they say 14 months. That’d be how long I can sustain.

But everyone is saying the right thing. My main doctor thinks I’ll be responding quickly in regards to a few symptoms. As of now, there are no plans to cancel the wedding, honeymoon, or anything of the sort.

Now with that being said, these optimistic outlooks were all before I was in the hospital for five days with a surprise pulmonary embolism. Turns out cancer can cause blood clots (had no idea) and my first bout with one put me in a mental and physical state I’ve never been in before.

Now I am living life with an oxygen machine, walking with a walker and being ushered to different medical offices in wheelchairs.

This life in the slow lane is not permanent, but it’s another detour that my life can take now. I am going to be on blood thinners for the rest of my life, and every calf impingement that may feel like a cramp could end up being another medical adventure.

I have a lot of changes coming. For the foreseeable future, I will be doing traditional Chemotherapy every other week, followed by 48 hours of Chemotherapy at home/on the road via fanny pack technology.

I will have that classic seven day pill counter on my dining room table to keep track of my drugs.

I am going to have a lot more people around me.

Since the news of my first official diagnosis, my parents have been up from Florida. My sisters have been with me hospital visits. This is going to be an adjustment for me. This is not a slight to people in general, but I don’t like them. I am an introvert. I like being alone, but I don’t like being lonely. I prefer having my background noise on working on whatever project I want. However, these days, the amount of noise and space in all my normal areas of respite have been altered.

It is just something else that I am going to need to adjust to. I am going to need to be able to ask for help because I can’t get myself out of a chair. I am unable to make my own food because standing up for too long makes me dizzy. I’m going to need to ask for help taking showers because I can’t get certain parts of my body wet.

I am going to learn how to ask for help, and not be stubborn. Wish me luck.

To all the people have helped me already, thank you. I know I’ve been a monster at times. A complete and total asshole. I’m quickly triggered and scared, which is not a good combo. To everyone who has helped me, and will continue to help me, thank you.

I need you now. And I’ll need you in the future. And here is to hoping the near and far future aren’t altered too much.

On Monday, April 29th, I was diagnosed with stage four Adenocarcinoma gastric cancer.

Today, Friday, May 10th, is my first day of Chemotherapy.

On Friday, July 5th, my fiancée and I will get married.

Stanko’s Stance may go on a hiatus, but it’ll be back.

17 Comments »

  1. I’m sure all of this is mind-blowing to you….There are a lot of people praying 🙏 and pulling for you…..you may not remember all of us, but we are a clan. We are fierce warriors….one for all and all for one!!

    Like

  2. You should really look into eastern medicine/alt treatments if they believe chemo won’t be the best. Order some graviola (soursop plant). Tons of studies about this shrinking cells and fighting cancer. Also dewormers like Ivermectin (I know it sounds like a conspiracy), but also a lot of cases of it killing tumors. Best of luck Stanko we’ll see you back producing soon

    Like

  3. You’re in great hands at Sloan Kettering My wife was diagnosed with a rare form of brain cancer in 2020 (only 1500 people diagnosed worldwide)Prognosis was grim and her future was uncertain at best before transferring her to MSK. We will be celebrating our 28th wedding anniversary next week cancer free. Positive Vibes Only 💪

    Like

  4. I’m a huge fan of your work Stanko! This sucks more than most things one can encounter in life- god bless you and those around you also enduring this. I wish you all the best and hope you beat this. Cancer fucking sucks and seems to hit those most undeserving, lost my mom three years ago. Be strong and know that you’ve impacted more people than you know. Keep up your passion for movies, as much as you can, be strong, but don’t be afraid to lean on those who love you.

    Like

  5. unlike others, I can imagine what you’re going through. I was diagnosed with stage III precursor t-cell lymphoblastic lymphoma on 10/1/2007. My kidneys were down to 6% function and by all outside measures, my prognosis did not look good. Your attitude and positivity will make a bigger impact on your cancer battle than anything else besides the chemo itself. I’ll never understand why these things happen to good people, particularly young people, but I do know that God has big plans for you. You just can’t see these plans or understand them right now.

    P.S. your best bet is to ignore all these morons giving keyboard advice on deworming medication and listen to the doctors who have devoted their lives and careers to provide the treatment plans for people like us. They know their shit.

    Like

  6. The Rife machine and other types of similar machines produce low energy waves. These waves are also called radio frequency electromagnetic fields. They have low energy compared to x-rays or radiotherapy which has high energy. The use of low energy waves as a treatment is less common, but there is some research on it.

    Rife and his supporters say that all medical conditions have an electromagnetic frequency. Rife treatment works by finding the frequency of the condition. An impulse of the same frequency is then used to kill or disable diseased cells.

    https://www.cancerresearchuk.org/about-cancer/treatment/complementary-alternative-therapies/individual-therapies/rife-machine-and-cancer

    Like

  7. I’m a 10 year Barstool fan and hearing this after what you have contributed made me a puddle. Stay strong Stanko, you may not know it but you have thousands if not millions on your side. Love always and you’ll be back to cooking in an apron in no time.

    Like

Leave a reply to ER Cancel reply